Add to ORKGThe latest synthetic strategies to prepare 2,2-bipyridine and its mono-substituted, symmetrical and unsymmetrical 3,3-, 4,4-, 5,5-, and 6,6-disubstituted derivatives are critically discussed and evaluated. Different coupling procedures to achieve new symmetrical and unsymmetrical functionalized 2,2-bipyridines, such as Stille-type, Negishi-type, and Suzuki-type cross-coupling reactions are discussed in detail. Moreover, condensation procedures that allow further variations are presented. The application of functional group transformations for access to additional groups is examined
International audienceCommercial 4,4'-bipyridine is a popular scaffold which is primarily employed a...
The scope of a flexible route to unsymmetrically functionalized bipyridines is described. Starting f...
The well-known reaction of 4'-chloro-2,2':6',2''-terpyridine with alkoxide nucleophiles leads to 4'-...
The latest synthetic strategies to prepare 2,2-bipyridine and its mono-substituted, symmetrical and ...
The 2,2'-bipyridine has been entitled as the most widely used ligand. Nowadays there is a large vari...
Stille-type cross-coupling procedures are utilized in order to prepare a variety of functionalized 2...
The sustained interest in the synthesis of new analogs of 2,2’- bipyridines is supported by the impo...
2,2'-Bipyridines and their appropriate N,N'-dioxides form a significant class of heteroaromatic comp...
Azine containing biaryls are ubiquitous scaffolds in many areas of chemistry, and efficient methods ...
In this contribution, Stille-type cross-coupling procedure is shown to be an easy and universal way ...
International audienceThe present review describes the homogenous catalytic methodologies for the sy...
International audienceNon-symmetrical chiral 4,4′-bipyridines have recently found interest in organo...
International audienceCommercial 4,4'-bipyridine is a popular scaffold which is primarily employed a...
The scope of a flexible route to unsymmetrically functionalized bipyridines is described. Starting f...
The well-known reaction of 4'-chloro-2,2':6',2''-terpyridine with alkoxide nucleophiles leads to 4'-...
The latest synthetic strategies to prepare 2,2-bipyridine and its mono-substituted, symmetrical and ...
The 2,2'-bipyridine has been entitled as the most widely used ligand. Nowadays there is a large vari...
Stille-type cross-coupling procedures are utilized in order to prepare a variety of functionalized 2...
The sustained interest in the synthesis of new analogs of 2,2’- bipyridines is supported by the impo...
2,2'-Bipyridines and their appropriate N,N'-dioxides form a significant class of heteroaromatic comp...
Azine containing biaryls are ubiquitous scaffolds in many areas of chemistry, and efficient methods ...
In this contribution, Stille-type cross-coupling procedure is shown to be an easy and universal way ...
International audienceThe present review describes the homogenous catalytic methodologies for the sy...
International audienceNon-symmetrical chiral 4,4′-bipyridines have recently found interest in organo...
International audienceCommercial 4,4'-bipyridine is a popular scaffold which is primarily employed a...
The scope of a flexible route to unsymmetrically functionalized bipyridines is described. Starting f...
The well-known reaction of 4'-chloro-2,2':6',2''-terpyridine with alkoxide nucleophiles leads to 4'-...